College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China.
Shandong Provincial Collaborative Innovation Center for Antiviral Traditional Chinese Medicine, Jinan 250355, China.
Viruses. 2018 Nov 30;10(12):679. doi: 10.3390/v10120679.
Influenza A viruses (IAV) carrying reporter genes provide a powerful tool to study viral infection and pathogenesis in vivo, however, incorporating a non-essential gene into the IAV genome often results in virus attenuation and genetic instability. Very few studies have systematically compared different reporter IAVs, and most optimization attempts seem to lack authentic directions. In this study, we evaluated the ratio of genome copies to the number of infectious unit of two reporter IAVs, PR8-NS1-Gluc and PR8-PB2-Gluc. As a result, PR8-NS1-Gluc and PR8-PB2-Gluc produced 41.4 and 3.8 genomes containing noninfectious particles respectively for every such particle produced by parental PR8 virus. RdRp assay demonstrated that modification of segment NS by inserting reporter genes can interfere with the replication competitive property of the corresponding vRNAs, and the balance of the 8 segments of the reporter IAVs were drastically impaired in infected cells. As a consequence, large amounts of NS-null noninfectious particles were produced during the PR8-NS1-Gluc packaging. In summary, we unravel a mechanism underlying attenuation of reporter IAVs, which suggests a new approach to restore infectivity and virulence by introducing extra mutations compensating for the impaired replication property of corresponding segments.
甲型流感病毒(IAV)携带报告基因,为研究病毒在体内的感染和发病机制提供了有力工具,然而,将非必需基因整合到 IAV 基因组中通常会导致病毒衰减和遗传不稳定。很少有研究系统比较不同的报告 IAV,并且大多数优化尝试似乎缺乏真实的方向。在本研究中,我们评估了两种报告 IAV(PR8-NS1-Gluc 和 PR8-PB2-Gluc)的基因组拷贝数与感染性单位数的比值。结果表明,PR8-NS1-Gluc 和 PR8-PB2-Gluc 产生的每个无感染性颗粒分别含有 41.4 和 3.8 个基因组,而亲本 PR8 病毒则产生 1 个这样的颗粒。RdRp 测定表明,通过插入报告基因修饰 NS 节段会干扰相应 vRNA 的复制竞争特性,并且感染细胞中报告 IAV 的 8 个节段的平衡严重受损。因此,在 PR8-NS1-Gluc 包装过程中会产生大量的 NS 缺失无感染性颗粒。总之,我们揭示了报告 IAV 衰减的机制,这为通过引入额外的突变来恢复感染性和毒力提供了一种新方法,这些突变可以补偿相应节段受损的复制特性。